A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005159



Internal ID71066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128311625..128311702hg38UCSC Ensembl
chr7:127951678..127951755hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488473
Supporting Variants
Samples
Known GenesRBM28
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005159
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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